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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25278생성일: 2026년 10월 26일

Water → 2-Cyclobutylmethylthio-4-(3-trifluoromethylpyrazolyl)benzonitrile

https://huagongshe.com/reaction/25278

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물(Bromomethyl)cyclobutaneHCID 2734658—
반응물HCID 178509603HCID 178509603—
용매DimethylformamideHCID 6228—
생성물2-Cyclobutylmethylthio-4-(3-trifluoromethylpyrazolyl)benzonitrileHCID 17850960521.6%

반응 단계

0.9 g (3.3 mmol) of 2-mercapto-4-(3-trifluoromethylpyrazolyl)benzonitrile, 0.5 g (3.3 mmol) of cyclobutylmethyl bromide and 0.55 g (4.0 mmol) of potassium carbonate were stirred in 5 ml of N,N-dimethylformamide at room temperature overnight. The resulting reaction mixture was poured into 50 ml of water and the organic matters were extracted with 20 ml of ethyl acetate twice. The ethyl acetate layers were combined, then washed with 30 ml of water twice and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 0.24 g of 2-cyclobutylmethylthio-4-(3-trifluoromethylpyrazolyl)benzonitrile (yield 21.2%) as a pale yellow powder (m.p. 102-103° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858639B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-109991864653475a9fb514957c60a928
출처 메모uspto-grants-2005_02